ProfileGDS1065 / 208682_s_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 79% 71% 77% 84% 74% 77% 84% 67% 75% 72% 76% 76% 79% 77% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1170.779
GSM24653Normal subject 2105.271
GSM24654Normal subject 3193.877
GSM24655A3243G-MELAS subject 114784
GSM24656A3243G-MELAS subject 213074
GSM24657A3243G-MELAS subject 3240.577
GSM24658A3243G-MELAS subject 4222.684
GSM24659A3243G-PEO subject 171.767
GSM24660A3243G-PEO subject 2114.675
GSM24661A3243G-PEO subject 379.772
GSM24662A3243G-PEO subject 4119.376
GSM24663mtDNA "Common"-deletion subject 1151.376
GSM24664mtDNA "Common"-deletion subject 2299.579
GSM24665mtDNA "Common"-deletion subject 3225.177
GSM24666mtDNA "Common"-deletion subject 4164.569